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编码人血小板糖蛋白 Ibβ 的基因的结构表征和染色体定位。

Structural characterization and chromosomal location of the gene encoding human platelet glycoprotein Ib beta.

作者信息

Yagi M, Edelhoff S, Disteche C M, Roth G J

机构信息

Hematology Section, Seattle Veterans Administration Medical Center, Washington 98108.

出版信息

J Biol Chem. 1994 Jul 1;269(26):17424-7.

PMID:8021244
Abstract

Human platelet glycoprotein Ib beta (GPIb beta) (M(r) 22,000) is part of the GPIb-V-IX system that constitutes the receptor for von Willebrand factor and mediates platelet adhesion in the arterial circulation. The four members of the receptor (GPs Ib alpha, Ib beta, V, and IX) share structural and functional features. Individually, GPIb beta contributes to surface expression of the receptor and participates in transmembrane signaling through phosphorylation of its intracellular domain. To define the structure of the GPIb beta gene, a cosmid clone from a human genomic library was analyzed. The transcriptional start site was located by both primer extension and the "anchored" polymerase chain reaction. Similar to the genes for Ib alpha, V, and IX, the Ib beta gene is compact with a single 274-base intron inserted into the 5' end of the open reading frame. The 5'-flanking region of the gene contains both GATA and ets sites that are also found in the 5' promoter regions of other described megakaryocyte/platelet genes. The GPIb beta gene was localized to chromosome 22q11.2 by fluorescence in situ hybridization. The GPIb beta gene has a simple structure, similar to that of other described megakaryocyte/platelet genes, including those of the GPIb-V-IX system.

摘要

人血小板糖蛋白Ibβ(GPIbβ)(分子量22,000)是GPIb-V-IX系统的一部分,该系统构成血管性血友病因子的受体并介导动脉循环中的血小板黏附。该受体的四个成员(糖蛋白Ibα、Ibβ、V和IX)具有结构和功能特征。单独来看,GPIbβ有助于受体的表面表达,并通过其胞内结构域的磷酸化参与跨膜信号传导。为了确定GPIbβ基因的结构,对来自人类基因组文库的一个黏粒克隆进行了分析。通过引物延伸和“锚定”聚合酶链反应确定了转录起始位点。与Ibα、V和IX的基因相似,Ibβ基因结构紧凑,一个274个碱基的单一内含子插入到开放阅读框的5'端。该基因的5'侧翼区域包含GATA和ets位点,在其他已描述的巨核细胞/血小板基因的5'启动子区域也能找到这些位点。通过荧光原位杂交将GPIbβ基因定位到22号染色体q11.2区。GPIbβ基因结构简单,与其他已描述的巨核细胞/血小板基因相似,包括GPIb-V-IX系统的那些基因。

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